药物输送
体内
结直肠癌
材料科学
活力测定
毒品携带者
纳米技术
MTT法
医学
药理学
癌症
化学
体外
内科学
生物化学
生物
生物技术
作者
Jinyan Shi,Zhiwei Ma,Hao Pan,Yang Liu,Yuqi Chu,Jinglei Wang,Lijiang Chen
标识
DOI:10.1080/02652048.2020.1797914
摘要
Aim In this study, 5-fluorouracil (5-FU) is delivered to target colon without the interference of mononuclear phagocyte system (MPS).Methods Outer membrane vesicles (OMVs) were used as the biological shield to disguise mesoporous silica (MSN) and 5-FU. OMVs-MSN-5-FU were prepared by high pressure co-extrusion, and characterised on the basis of size, drug loading, transmission electron microscope, infra-red spectroscopy, differential scanning calorimetry, thermal gravity analysis, % in vitro release, MTT assay, cell uptake and in vivo imaging.Results OMVs-MSN-5-FU with −18.22 ± 0.17 mV zeta potential and 90.4 ± 9.1 nm size were used for oral treatment of colon cancer. Drug loading of the drug was 50.22%±0.17 (w/w). The cumulative release of OMVs-MSN-5-FU reached 75.07%±0.94 in tumour microenvironment. The percentage of cell viability of OMVs-MSN-5-FU was 33.75%±2.73. In vivo experiments results confirmed that OMVs-MSN-5-FU could be taken up by colon cancer cells.Conclusions The study provided a promising nano platform for the targeting treatment of colon cancer.
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